CI

At a glance

ClinicalIndex Comparison Record
Phase 1Completed· 107 enrolled
Drug / intervention
LGX818drug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT01436656
NCT01436656Phase 1Completed

A Phase I, Multicenter, Open-label, Dose-escalation Study of Oral LGX818 in Adult Patients With Locally Advanced or Metastatic BRAF Mutant Melanoma

Pfizer·interventional·Posted Sep 20, 2011·Updated Oct 28, 2024

In Brief

A Phase 1 clinical trial evaluating LGX818 for Melanoma and Metastatic Colorectal Cancer. Completed, enrolled 107 participants across 24 sites in 7 countries.

Detailed Summary

CLGX818X2101 is a first-time in-human, phase I study to establish the maximum tolerated dose (MTD) and/or recommended phase 2 dose (RP2D) of daily administered LGX818 (daily, twice daily and/or every-other-day), a RAF kinase inhibitor. Patients with locally advanced or metastatic melanoma harboring the BRAF V600 mutation (during dose escalation phase and expansion phase) and patients with metastatic colorectal cancer harboring the BRAF V600 mutation (during the expansion phase) will be enrolled. The study consists of a dose escalation part were cohorts of patients will receive escalating oral doses of LGX818, followed by a safety dose expansion part were patients will be treated with oral dose of LGX818 given at the MTD or RP2D.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesAustralia, France, Japan, Norway, Spain, Switzerland, United States
Collaborators--

Timeline

Phase 1CompletedFinished
201220132014201520162017201820192020202120222023202420252026
First PostedSep 20, 2011
Enrollment StartSep 5, 2011
Primary CompletionOct 1, 2012
Study CompletionNov 7, 2022
TodayJul 2, 2026
Enrollment to primary: 1.1 yearsPosted 14.8 years ago

Interventions

LGX818drug